Ronicke M, Sollfrank L, Vitus MV, Walter LJ, Krieter M, Moelleken M, Dissemond J, Schultz E, Lauffer F, von den Driesch P, and Erfurt-Berge C
Background: Pyoderma gangrenosum (PG) is rare neutrophil skin disease causing painful, progressively enlarging ulcers. Among the treatment options, intravenous immunoglobulin (IVIG) is a therapy of first choice for paraneoplastic PG. Otherwise, it is used in therapy-refractory courses., Objective: To assess the efficacy and safety of IVIG therapy in patients with PG., Methods: A retrospective chart review for patients in five dermatologic wound centres in Germany was performed., Results: Overall, 81 patients were included. IVIG was used as adjunct therapy with (methyl-) prednisolone and/or a steroid sparing therapy in 77 (95.1%) cases. Response to treatment (combined complete and partial, defined as tendency to heal and cessation of lesion progression, respectively) was 49.3% 1 month after initiation of IVIG. In total 18.8% had a complete response after 6 months. Statistically significantly higher response rates were observed in patients with diabetes mellitus and thyroid disease [odds ratio (OR) 3.49, confidence interval (CI) 1.13-10.80 and OR 6.64, CI 1.01-43.57, respectively]. Patients with solid malignancy tended to have better response (OR 4.36, CI 0.79-23.91). A higher IVIG dose was also associated with a tendency towards better response rates (OR 2.70, CI 0.84-8.63). In total, 1 (1.2%) severe adverse event (myocardial infarction with consequent death) was observed as well as three moderate adverse events, with two thromboembolic events (2.5%) and one acute kidney injury (1.2%). Other adverse events were mild or unlikely to be associated with IVIG therapy, with 14 events in 10 patients overall (12.3%)., Conclusions: This multicentre retrospective study shows the important role of adjunctive IVIG therapy in patients with PG with recalcitrant courses. Identifying subgroups with a higher probability of response could improve future response rates and save patients from ineffective treatment and potential adverse events., Competing Interests: Declarations. Funding: Open Access funding enabled and organized by Projekt DEAL. M.R. and L.S. were funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—493624887 (Clinician Scientist Program NOTICE). Conflicts of interest: None declared. Ethical approval: Reviewed and approved by the local ethics committee (ethics committee of the Friedrich-Alexander-Universität Erlangen-Nürnberg), # 23-430-Br. Data availability statement: The data that support the findings of this study are available from the corresponding author upon reasonable request. Patient consent to participate: Not applicable due to retrospective study design. Patient consent to publish: Not applicable due to retrospective study design. Code availability: Not applicable. Author contributions: M.R. carried out conceptualization, data curation, investigation, funding acquisition, methodology, project administration, visualization and writing—original draft preparation; L.S. carried out conceptualization, data curation, investigation, funding acquisition, methodology and writing—review and editing; M.V., L.W., M.K. and M.M. carried out data curation, investigation and writing—review and editing; J.D., E.S., F.L. and P.v.d.D. carried out supervision and writing—review and editing; C.E.-B. carried out conceptualization, supervision and writing—review and editing., (© 2024. The Author(s).)